Deng A Y, Rapp J P
Department of Physiology and Molecular Medicine, Medical College of Ohio, Toledo 43699, USA.
J Clin Invest. 1995 May;95(5):2170-7. doi: 10.1172/JCI117906.
Alleles of the inducible nitric oxide synthase locus (Nos2) cosegregated highly significantly (P < 0.0001) with blood pressure in an F2 population [F2(S x MNS), n = 171] derived from a cross of inbred Dahl salt-sensitive (S) rats with Milan normotensive rats (MNS). In contrast, alleles at the constitutive brain nitric oxide synthase locus (Nos1) did not cosegregate with blood pressure in several F2 populations. Nos2 was mapped on rat chromosome 10. Nine genetic markers, including the angiotensin-converting enzyme (Ace) and Nos2 loci spanning roughly 46 cM on rat chromosome 10, all cosegregated strongly with blood pressure in the F2(S x MNS) population. Nos2 showed the highest LOD score of 6.3. Ace and Nos2 are 30 cM apart. In an F2 population [F2(S x WKY), n = 159] derived from a cross of S rats with Wistar-Kyoto (WKY) rats, Nos2 alleles did (P = 0.0070), but Ace alleles did not (P = 0.91), cosegregate with blood pressure. We conclude that the Nos2 locus rather than the Nos1 locus is a candidate for influencing blood pressure in the S rat. There are probably two separate but linked quantitative trait loci (QTL) for blood pressure on rat chromosome 10, one marked by Ace and the other marked by Nos2. In F2(S x MNS) functionally variant alleles at both QTL influence blood pressure, but in F2(S x WKY) only the QTL marked by Nos2 is segregating alleles influencing blood pressure.
在由近交系 Dahl 盐敏感(S)大鼠与米兰正常血压大鼠(MNS)杂交产生的 F2 群体[F2(S×MNS),n = 171]中,诱导型一氧化氮合酶基因座(Nos2)的等位基因与血压的共分离具有极显著意义(P < 0.0001)。相比之下,在几个 F2 群体中,组成型脑一氧化氮合酶基因座(Nos1)的等位基因与血压没有共分离。Nos2 被定位在大鼠第 10 号染色体上。包括血管紧张素转换酶(Ace)和 Nos2 基因座在内的 9 个遗传标记在大鼠第 10 号染色体上跨度约 46 cM,在 F2(S×MNS)群体中均与血压强烈共分离。Nos2 显示出最高的 LOD 分数为 6.3。Ace 和 Nos2 相距 30 cM。在由 S 大鼠与Wistar - Kyoto(WKY)大鼠杂交产生的 F2 群体[F2(S×WKY),n = 159]中,Nos2 等位基因与血压共分离(P = 0.0070),但 Ace 等位基因与血压没有共分离(P = 0.91)。我们得出结论,在 S 大鼠中,影响血压的候选基因是 Nos2 基因座而非 Nos1 基因座。在大鼠第 10 号染色体上可能存在两个独立但连锁的血压数量性状基因座(QTL),一个由 Ace 标记,另一个由 Nos2 标记。在 F2(S×MNS)中,两个 QTL 上的功能变异等位基因均影响血压,但在 F2(S×WKY)中,只有由 Nos2 标记的 QTL 分离出影响血压的等位基因。